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dc.contributor.authorKopka, Paweł
dc.contributor.authorBliźniewska, Katarzyna
dc.contributor.authorTreliński, Jacek
dc.contributor.authorChojnowski, Krzysztof
dc.contributor.authorSicińska, Paulina
dc.contributor.authorDuchnowicz, Piotr
dc.contributor.authorBukowska, Bożena
dc.date.accessioned2021-10-15T08:08:44Z
dc.date.available2021-10-15T08:08:44Z
dc.date.issued2020
dc.identifier.issn0032-5449
dc.identifier.urihttp://hdl.handle.net/11089/39391
dc.description.abstractAim: Polycythemia vera (PV) and essential thrombocythemia (ET) are Philadelphia–negative myeloproliferative neoplasms with documented apoptosis impairment at the level of hematopoietic stem cell. However, so far no study has evaluated apoptosis of circulating blood neoplastic cells, including the suicidal death of erythrocytes – eryptosis. Material/Methods: Erythrocytes from 61 patients (24 PV and 37 ET) naïve to and treated with hydroxyurea (HU) and 13 healthy individuals were analysed using flow cytometry to quantify phosphatidylserine (PS) externalization from Annexin-V-binding, calpain activity from 7-amino-4-chloromethylcoumarin (CMAC)-fluorescence, cell volume from forward scattered light (FSC) and cell shape from side scattered light (SSC). Results: Significantly increased levels of calpain activity and PS exposure were observed in both ET and PV naïve patients, indicating enhanced eryptosis. Among HU-treated patients, a significant increase in calpain activity in the ET group and a decrease in the PV group were observed compared to patients without cytoreductive therapy. Among PV patients, FSC was substantially higher in the HU-treated group than in the naïve group, whereas no significant differences were found between HU-treated and HU-naïve groups of ET patients. Conclusions: The enhanced eryptosis in ET and PV patients may be a form of systemic compensation of the pathological bone marrow overproduction of erythrocytes. HU, the basic cytoreductive drug used in ET and PV, may affect eryptosis in PV and ET in different ways depending on disease. The JAK2V617F mutation was not observed to have any effect on eryptosis in ET.pl_PL
dc.description.sponsorshipThe study was supported by Medical University of Lodz grant number: 502-03/1-093-02/502-14-347.pl_PL
dc.language.isoenpl_PL
dc.publisherSciendo, De Gruyter Poland Sp. z o.o.; Instytut Immunologii i Terapii Doświadczalnej PANpl_PL
dc.relation.ispartofseriesPostępy Higieny i Medycyny Doświadczalnej / Advances in Hygiene and Experimental Medicine;74
dc.rightsUznanie autorstwa-Użycie niekomercyjne 4.0 Międzynarodowe*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.subjectEssential thrombocythemiapl_PL
dc.subjectPolycythemia verapl_PL
dc.subjectEryptosispl_PL
dc.subjectHydroxyureapl_PL
dc.subjectJAK2V617F mutationpl_PL
dc.titleEryptosis in polycythemia vera and essential thrombocythemiapl_PL
dc.typeArticlepl_PL
dc.page.number69-76pl_PL
dc.contributor.authorAffiliationDepartment of Hemostasis Disorders, Medical University of Lodz, Department of Hematology, Copernicus Memorial Hospital, Lodz, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Hemostasis Disorders, Medical University of Lodz, Department of Hematology, Copernicus Memorial Hospital, Lodz, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Hemostasis Disorders, Medical University of Lodz, Department of Hematology, Copernicus Memorial Hospital, Lodz, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Hemostasis Disorders, Medical University of Lodz, Department of Hematology, Copernicus Memorial Hospital, Lodz, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Environmental Pollution Biophysics, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Environmental Pollution Biophysics, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Environmental Pollution Biophysics, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Polandpl_PL
dc.identifier.eissn1732-2693
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dc.identifier.doi10.5604/01.3001.0014.0855
dc.disciplinenauki biologicznepl_PL


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